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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095458copy number variation4nstd102humanUncertain significance GRCh37 chr19: 10,828,919-13,482,613 , GRCh38.p12 chr19: 10,718,243-13,371,799 WDR83OS, RPL10P16, 140 more genes
    nsv7062606inversion1nstd229human GRCh38 chr19: 10,024,335-10,946,724 , GRCh37.p13 chr19: 10,135,011-11,057,400 FDX2, ICAM4, 48 more genes
    nsv7061047inversion1nstd229human GRCh38 chr19: 10,123,796-11,885,300 , GRCh37.p13 chr19: 10,234,472-11,996,115 QTRT1, ZNF653, 82 more genes
    nsv7013931copy number variation1nstd229human GRCh38 chr19: 10,794,301-10,934,700 , GRCh37.p13 chr19: 10,904,977-11,045,376 DNM2, CARM1, 6 more genes
    nsv6998259copy number variation1nstd229human GRCh38 chr19: 10,046,601-11,033,768 , GRCh37.p13 chr19: 10,157,277-11,144,444 MRPL4, QTRT1, 49 more genes
    nsv6520341copy number variation1nstd223human GRCh38 chr19: 10,883,935-11,045,237 , GRCh37.p13 chr19: 10,994,611-11,155,913 TIMM29, CARM1, 3 more genes
    nsv6291543copy number variation1nstd102humanUncertain significance GRCh37 chr19: 9,941,033-11,739,567 , GRCh38.p12 chr19: 9,830,357-11,628,752 KRI1, SHFL, 88 more genes
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv5381193copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,912,954-11,200,309 , GRCh38.p12 chr19: 10,802,278-11,089,633 SMARCA4, RN7SL192P, 10 more genes
    nsv5321778copy number variation1nstd204human GRCh37.p13 chr19: 11,035,706-11,044,926 , GRCh38.p13 chr19: 10,925,030-10,934,250 TIMM29, YIPF2
    nsv5298909copy number variation1nstd204human GRCh38.p13 chr19: 10,842,201-11,593,800 , GRCh37.p13 chr19: 10,952,877-11,704,615 KANK2, RPL18AP13, 35 more genes
    nsv5287330copy number variation1nstd204human GRCh38.p13 chr19: 10,335,601-11,755,400 , GRCh37.p13 chr19: 10,446,277-11,866,215 AP1M2, C19orf38, 64 more genes
    nsv5286396copy number variation1nstd204human GRCh38.p13 chr19: 10,925,158-10,929,187 , GRCh37.p13 chr19: 11,035,834-11,039,863 YIPF2, TIMM29
    nsv5285730copy number variation1nstd204human GRCh38.p13 chr19: 10,872,301-10,941,400 , GRCh37.p13 chr19: 10,982,977-11,052,076 TIMM29, CARM1, 1 more genes
    nsv5281589copy number variation1nstd204human GRCh38.p13 chr19: 10,925,001-10,934,300 , GRCh37.p13 chr19: 11,035,677-11,044,976 TIMM29, YIPF2
    nsv4860231copy number variation1nstd200human GRCh37 chr19: 11,035,716-11,044,918 , GRCh38.p12 chr19: 10,925,040-10,934,242 YIPF2, TIMM29
    nsv4729806copy number variation1nstd102humanPathogenic GRCh37 chr19: 10,957,601-11,672,041 , GRCh38.p12 chr19: 10,846,925-11,561,226 DOCK6-AS1, C19orf38, 32 more genes
    nsv4685775copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 SLC44A2, ZNF833P, 114 more genes
    nsv4676283copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,632,623-11,135,294 , GRCh38.p12 chr19: 10,521,947-11,024,618 ATG4D, RN7SL192P, 21 more genes
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